Vaida joined the Industrial Policies team in March 2023. As a Manager In Vitro Diagnostics, Vaida is contributing to MedTech Europe’s work on the implementation of the In Vitro Diagnostic Medical Devices Regulation. She is currently coordinating the Post-Market Surveillance and Vigilance working group (IVD and MD) and IVD Labelling working group.
Vaida holds a BSc in Public Health and MSc in Public Policy from Maastricht University. Prior to joining MedTech Europe, she worked at Medtronic as an Associate Regulatory Operations Specialist, with special focus on the implementation of the Economic Operators’ requirements under the new EU Medical Device Regulation (MDR).
Vaida is a Lithuanian national. She speaks fluent Lithuanian and English, intermediate Dutch, and Russian. Outside of work, she does lots of yoga and loves travelling.
